Canonical Allele Identifier: CA394876298

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16155028-C-T
• MyVariant Identifiers: chr16:g.16248885C>T (hg19) ; chr16:g.16155028C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155028C>T , CM000678.2:g.16155028C>T	GRCh38
NC_000016.9:g.16248885C>T , CM000678.1:g.16248885C>T	GRCh37
NC_000016.8:g.16156386C>T	NCBI36
NG_007558.2:g.73444G>A
NG_007558.3:g.73590G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.749G>A
ENST00000622290.5:c.*58G>A	ENSP00000483331.2:n.*58G>A
ENST00000205557.12:c.3886G>A MANE Select	ENSP00000205557.7:p.Gly1296Ser
ENST00000640696.1:c.700G>A	ENSP00000492197.1:p.Gly234Ser
ENST00000205557.11:c.3886G>A	ENSP00000205557.7:p.Gly1296Ser
ENST00000456970.6:c.3511G>A	ENSP00000405002.2:n.3511G>A
ENST00000576204.5:n.749G>A
ENST00000622290.4:c.*1095G>A	ENSP00000483331.1:n.*1095G>A
NM_001171.5:c.3886G>A	NP_001162.4:p.Gly1296Ser
XM_011522479.1:c.3853G>A	XP_011520781.1:p.Gly1285Ser
XM_011522480.1:c.3544G>A	XP_011520782.1:p.Gly1182Ser
XM_011522481.1:c.3544G>A	XP_011520783.1:p.Gly1182Ser
XR_932836.1:n.4184G>A
XR_932837.1:n.3922G>A
XR_932838.1:n.3985G>A
XR_933134.1:n.539-4753C>T
NM_001351800.1:c.3544G>A	NP_001338729.1:p.Gly1182Ser
NR_147784.1:n.3548G>A
XM_011522479.2:c.3853G>A	XP_011520781.1:p.Gly1285Ser
XM_011522481.3:c.3544G>A	XP_011520783.1:p.Gly1182Ser
XM_017023212.1:c.3718G>A	XP_016878701.1:p.Gly1240Ser
XM_024450261.1:c.3922G>A	XP_024306029.1:p.Gly1308Ser
XR_932836.2:n.4130G>A
XR_932837.3:n.3867G>A
XR_932838.3:n.3930G>A
NM_001171.6:c.3886G>A MANE Select	NP_001162.5:p.Gly1296Ser